# Commission Regulation (EU) No 544/2011 of 10 June 2011 implementing Regulation (EC) No 1107/2009 of the European Parliament and of the Council as regards the data requirements for active substances (Text with EEA relevance) (repealed), Division: Test guidelines

Extent: E+W+S+N.I.

The following test guidelines are acceptable:
Annex to Regulation (EC) No 440/2008, Method B 12 — In vivo mammalian erythrocyte micronucleus test,
Annex to Regulation (EC) No 440/2008, Method B 24— Mouse spot test,
Annex to Regulation (EC) No 440/2008, Method B 11 — In vivo Mammalian Bone-Marrow chromosome aberration test.

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Source: https://www.legislation.gov.uk/eur/2011/544/annex/part/A/division/5/division/5.4/division/5.4.2/division/2 (the official version)
Page: https://openlegislation.uk/eu-regulation-2011-544/annex/part-A/division-5/division-5.4/division-5.4.2/division-2
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.